Canonical Allele Identifier: CA2147122455

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74611617G= , CM000676.2:g.74611617G=	GRCh38
NC_000014.8:g.75078320G= , CM000676.1:g.75078320G=	GRCh37
NC_000014.7:g.74148073G=	NCBI36
NG_021486.1:g.5715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.328C= MANE Select	ENSP00000261978.4:p.Gln110=
ENST00000261978.8:c.328C=	ENSP00000261978.4:p.Gln110=
ENST00000553939.5:c.328C=	ENSP00000452110.1:p.Gln110=
ENST00000556690.5:c.328C=	ENSP00000451477.1:p.Gln110=
ENST00000557425.1:n.123+429C=
NM_000428.2:c.328C=	NP_000419.1:p.Gln110=
XM_011536765.1:c.328C=	XP_011535067.1:p.Gln110=
XM_011536767.1:c.11+6967C=	XP_011535069.1:n.11+6967C=
XM_011536765.2:c.328C=	XP_011535067.1:p.Gln110=
NM_000428.3:c.328C= MANE Select	NP_000419.1:p.Gln110=